Canonical Allele Identifier: PA2830203911
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32141Cys
CA1985480
NM_133378.4:c.96421C>T